Arun Kumar Kondadi

1.2k total citations
19 papers, 817 citations indexed

About

Arun Kumar Kondadi is a scholar working on Molecular Biology, Clinical Biochemistry and Cancer Research. According to data from OpenAlex, Arun Kumar Kondadi has authored 19 papers receiving a total of 817 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 3 papers in Cancer Research. Recurrent topics in Arun Kumar Kondadi's work include Mitochondrial Function and Pathology (14 papers), ATP Synthase and ATPases Research (12 papers) and Metabolism and Genetic Disorders (10 papers). Arun Kumar Kondadi is often cited by papers focused on Mitochondrial Function and Pathology (14 papers), ATP Synthase and ATPases Research (12 papers) and Metabolism and Genetic Disorders (10 papers). Arun Kumar Kondadi collaborates with scholars based in Germany, United States and Lebanon. Arun Kumar Kondadi's co-authors include Andreas S. Reichert, Ruchika Anand, Dane M. Wolf, Orian S. Shirihai, Marc Liesa, Mayuko Segawa, David B. Shackelford, Alexander M. van der Bliek, Sean T. Bailey and Jennifer Urbach and has published in prestigious journals such as Nature Communications, The EMBO Journal and PLoS ONE.

In The Last Decade

Arun Kumar Kondadi

19 papers receiving 811 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Arun Kumar Kondadi Germany 11 722 232 95 69 56 19 817
Mayuko Segawa United States 9 593 0.8× 152 0.7× 78 0.8× 86 1.2× 41 0.7× 12 715
Ralf M. Zerbes Germany 12 819 1.1× 292 1.3× 87 0.9× 70 1.0× 34 0.6× 15 912
Markus Deckers Germany 20 1.3k 1.9× 270 1.2× 95 1.0× 93 1.3× 56 1.0× 25 1.5k
Florence Malka France 8 894 1.2× 351 1.5× 156 1.6× 103 1.5× 52 0.9× 10 997
Inge Kühl France 13 1.1k 1.5× 320 1.4× 85 0.9× 57 0.8× 48 0.9× 21 1.2k
Valentina Strecker Germany 12 560 0.8× 181 0.8× 47 0.5× 31 0.4× 31 0.6× 15 666
Carsten Bornhövd Germany 7 1.1k 1.5× 277 1.2× 117 1.2× 70 1.0× 82 1.5× 7 1.2k
Zuzana Technikova-Dobrova Italy 14 830 1.1× 176 0.8× 137 1.4× 39 0.6× 81 1.4× 16 908
Rajarshi Chakrabarti United States 12 504 0.7× 102 0.4× 64 0.7× 75 1.1× 78 1.4× 18 687
Alena Vojtı́šková Czechia 14 498 0.7× 167 0.7× 98 1.0× 33 0.5× 46 0.8× 15 639

Countries citing papers authored by Arun Kumar Kondadi

Since Specialization
Citations

This map shows the geographic impact of Arun Kumar Kondadi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Arun Kumar Kondadi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arun Kumar Kondadi more than expected).

Fields of papers citing papers by Arun Kumar Kondadi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arun Kumar Kondadi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Arun Kumar Kondadi. The network helps show where Arun Kumar Kondadi may publish in the future.

Co-authorship network of co-authors of Arun Kumar Kondadi

This figure shows the co-authorship network connecting the top 25 collaborators of Arun Kumar Kondadi. A scholar is included among the top collaborators of Arun Kumar Kondadi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Arun Kumar Kondadi. Arun Kumar Kondadi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Westhoff, Philipp, Anja Stefanski, Patrick Petzsch, et al.. (2024). Mitochondrial apolipoprotein MIC26 is a metabolic rheostat regulating central cellular fuel pathways. Life Science Alliance. 7(12). e202403038–e202403038. 2 indexed citations
2.
Kondadi, Arun Kumar & Andreas S. Reichert. (2024). Mitochondrial Dynamics at Different Levels: From Cristae Dynamics to Interorganellar Cross Talk. Annual Review of Biophysics. 53(1). 147–168. 23 indexed citations
3.
Urbach, Jennifer, et al.. (2024). SLP2 and MIC13 synergistically coordinate MICOS assembly and crista junction formation. iScience. 27(12). 111467–111467. 3 indexed citations
4.
Drießen, Marc D., Bengt‐Frederik Belgardt, Michael Roden, et al.. (2023). MIC26 and MIC27 are bona fide subunits of the MICOS complex in mitochondria and do not exist as glycosylated apolipoproteins. PLoS ONE. 18(6). e0286756–e0286756. 4 indexed citations
5.
Montfort, Claudia von, Arun Kumar Kondadi, C. Wenzel, et al.. (2023). Involvement of necroptosis in the selective toxicity of the natural compound (±) gossypol on squamous skin cancer cells in vitro. Archives of Toxicology. 97(7). 1997–2014. 2 indexed citations
6.
Montfort, Claudia von, C. Wenzel, Arun Kumar Kondadi, et al.. (2023). The Antimalarial Drug Artesunate Mediates Selective Cytotoxicity by Upregulating HO-1 in Melanoma Cells. Biomedicines. 11(9). 2393–2393. 4 indexed citations
7.
Hänsch, Sebastian, et al.. (2023). Cristae dynamics is modulated in bioenergetically compromised mitochondria. Life Science Alliance. 7(2). e202302386–e202302386. 10 indexed citations
8.
Krapp, Adriana R., Andrea M. J. Weiner, Hannes M. Beyer, et al.. (2023). NERNST: a genetically-encoded ratiometric non-destructive sensing tool to estimate NADP(H) redox status in bacterial, plant and animal systems. Nature Communications. 14(1). 3277–3277. 20 indexed citations
9.
Kurban, Mazen, et al.. (2023). A X‐linked nonsense APOO/MIC26 variant causes a lethal mitochondrial disease with progeria‐like phenotypes. Clinical Genetics. 104(6). 659–668. 8 indexed citations
10.
Urbach, Jennifer, et al.. (2021). Conserved GxxxG and WN motifs of MIC13 are essential for bridging two MICOS subcomplexes. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1863(12). 183683–183683. 8 indexed citations
11.
Kondadi, Arun Kumar, et al.. (2021). The BH3 mimetic (±) gossypol induces ROS-independent apoptosis and mitochondrial dysfunction in human A375 melanoma cells in vitro. Archives of Toxicology. 95(4). 1349–1365. 15 indexed citations
12.
Anand, Ruchika, Andreas S. Reichert, & Arun Kumar Kondadi. (2021). Emerging Roles of the MICOS Complex in Cristae Dynamics and Biogenesis. Biology. 10(7). 600–600. 46 indexed citations
13.
Kondadi, Arun Kumar, Ruchika Anand, Sebastian Hänsch, et al.. (2020). Cristae undergo continuous cycles of membrane remodelling in a MICOS ‐dependent manner. EMBO Reports. 21(3). e49776–e49776. 121 indexed citations
14.
Anand, Ruchika, Arun Kumar Kondadi, Julia Riedel, et al.. (2020). MIC26 and MIC27 cooperate to regulate cardiolipin levels and the landscape of OXPHOS complexes. Life Science Alliance. 3(10). e202000711–e202000711. 43 indexed citations
15.
Kondadi, Arun Kumar, Ruchika Anand, & Andreas S. Reichert. (2020). Cristae Membrane Dynamics – A Paradigm Change. Trends in Cell Biology. 30(12). 923–936. 111 indexed citations
16.
Wolf, Dane M., Mayuko Segawa, Arun Kumar Kondadi, et al.. (2019). Individual cristae within the same mitochondrion display different membrane potentials and are functionally independent. The EMBO Journal. 38(22). e101056–e101056. 234 indexed citations
17.
Kondadi, Arun Kumar, Ruchika Anand, & Andreas S. Reichert. (2019). Functional Interplay between Cristae Biogenesis, Mitochondrial Dynamics and Mitochondrial DNA Integrity. International Journal of Molecular Sciences. 20(17). 4311–4311. 65 indexed citations
18.
Danhauser, Katharina, Annette Seibt, Özer Degistirici, et al.. (2017). Modulation of oxidative phosphorylation and redox homeostasis in mitochondrial NDUFS4 deficiency via mesenchymal stem cells. Stem Cell Research & Therapy. 8(1). 150–150. 34 indexed citations
19.
Kondadi, Arun Kumar, Shaomeng Wang, Sara Montagner, et al.. (2014). Loss of the m-AAA protease subunit AFG3L2 causes mitochondrial transport defects and tau hyperphosphorylation. The EMBO Journal. 33(9). 1011–1026. 64 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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